Canonical Allele Identifier: CA344032881

Gene: CRB1

Linked Data

• gnomAD v4: 1-197421737-C-A
• COSMIC: COSM4474267 ; COSM4474268
• MyVariant Identifiers: chr1:g.197390867C>A (hg19) ; chr1:g.197421737C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197421737C>A , CM000663.2:g.197421737C>A	GRCh38
NC_000001.10:g.197390867C>A , CM000663.1:g.197390867C>A	GRCh37
NC_000001.9:g.195657490C>A	NCBI36
NG_008483.1:g.158460C>A
NG_008483.2:g.225276C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.1909C>A MANE Select	ENSP00000356370.3:p.Pro637Thr
ENST00000638467.1:c.1909C>A	ENSP00000491102.1:p.Pro637Thr
ENST00000681519.1:c.790C>A	ENSP00000505267.1:p.Pro264Thr
ENST00000367397.1:c.52C>A	ENSP00000356367.1:p.Pro18Thr
ENST00000367399.6:c.1573C>A	ENSP00000356369.2:p.Pro525Thr
ENST00000367400.7:c.1909C>A	ENSP00000356370.3:p.Pro637Thr
ENST00000484075.5:c.1909C>A	ENSP00000433932.1:p.Pro637Thr
ENST00000535699.5:c.1702C>A	ENSP00000438786.1:p.Pro568Thr
ENST00000538660.5:c.1909C>A	ENSP00000438091.1:p.Pro637Thr
NM_001193640.1:c.1573C>A	NP_001180569.1:p.Pro525Thr
NM_001257965.1:c.1702C>A	NP_001244894.1:p.Pro568Thr
NM_001257966.1:c.1909C>A	NP_001244895.1:p.Pro637Thr
NM_201253.2:c.1909C>A	NP_957705.1:p.Pro637Thr
NR_047563.1:n.1923-13C>A
NR_047564.1:n.2118C>A
XM_011509365.1:c.1909C>A	XP_011507667.1:p.Pro637Thr
XM_011509366.1:c.1909C>A	XP_011507668.1:p.Pro637Thr
XM_011509367.1:c.1909C>A	XP_011507669.1:p.Pro637Thr
XM_011509368.1:c.1327C>A	XP_011507670.1:p.Pro443Thr
XM_011509369.1:c.352C>A	XP_011507671.1:p.Pro118Thr
XM_011509365.2:c.1909C>A	XP_011507667.1:p.Pro637Thr
XM_011509369.2:c.352C>A	XP_011507671.1:p.Pro118Thr
XM_017000851.1:c.1066C>A	XP_016856340.1:p.Pro356Thr
XM_017000852.1:c.1909C>A	XP_016856341.1:p.Pro637Thr
NM_201253.3:c.1909C>A MANE Select	NP_957705.1:p.Pro637Thr
NM_001193640.2:c.1573C>A	NP_001180569.1:p.Pro525Thr
NM_001257965.2:c.1702C>A	NP_001244894.1:p.Pro568Thr
NR_047563.2:n.1875-13C>A
NR_047564.2:n.2070C>A
NM_001257966.2:c.1909C>A	NP_001244895.1:p.Pro637Thr